检索结果-内蒙古大学图书馆

您好，读者！请登录

内蒙古大学图书馆

首页
概况
党建
资源
服务
科研支持
- 论文收录引用证明
- 科技查新
知识产权
档案馆
帮助

咨询与建议

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

您的常用邮箱：*

您的手机号码：*

问题描述：

当前已输入0个字，您还可以输入200个字

全部搜索
期刊论文
图书
学位论文
标准
纸本馆藏
外文资源发现
数据库导航
超星发现

高级检索

时间限定

出版年份：

文献类型

图书期刊文献学位论文多媒体

馆藏选择

电子馆藏纸本馆藏

核心期刊

全部期刊 SCI 收录期刊 SSCI 收录期刊 EI 收录期刊 CSCD 收录期刊 CSSCI 收录期刊

语言

中文英文

文献类型

期刊文献图书学位论文标准纸本馆藏

帮助

文字说明：

T=题名（书名、题名），A=作者（责任者），K=主题词，P=出版物名称，PU=出版社名称，O=机构（作者单位、学位授予单位、专利申请人），L=中图分类号，C=学科分类号，U=全部字段，Y=年（出版发行年、学位年度、标准发布年）

检索规则说明：

AND代表“并且”；OR代表“或者”；NOT代表“不包含”；(注意必须大写,运算符两边需空一格)

检索范例：

范例一：(K=图书馆学 OR K=情报学) AND A=范并思 AND Y=1982-2016
范例二：P=计算机应用与软件 AND (U=C++ OR U=Basic) NOT K=Visual AND Y=2011-2016

分类表

所选分类

>> <<

限定检索结果

文献类型

1,138 篇 会议
346 篇 期刊文献
15 册 图书

馆藏范围

1,499 篇 电子文献
0 种 纸本馆藏

日期分布

学科分类号

739 篇 工学
- 605 篇 计算机科学与技术...
- 353 篇 电气工程
- 158 篇 软件工程
- 144 篇 生物工程
- 126 篇 生物医学工程（可授...
- 67 篇 控制科学与工程
- 58 篇 化学工程与技术
- 41 篇 信息与通信工程
- 11 篇 机械工程
- 8 篇 材料科学与工程（可...
- 8 篇 电子科学与技术（可...
- 7 篇 光学工程
- 7 篇 仪器科学与技术
- 6 篇 交通运输工程
- 5 篇 安全科学与工程
- 4 篇 冶金工程
566 篇 理学
- 510 篇 生物学
- 346 篇 数学
- 295 篇 统计学（可授理学、...
- 61 篇 化学
- 27 篇 系统科学
- 21 篇 物理学
98 篇 管理学
- 66 篇 管理科学与工程(可...
- 35 篇 图书情报与档案管...
- 9 篇 工商管理
73 篇 医学
- 63 篇 基础医学(可授医学...
- 35 篇 临床医学
- 24 篇 药学(可授医学、理...
- 10 篇 公共卫生与预防医...
35 篇 农学
- 32 篇 作物学
3 篇 法学
3 篇 教育学
2 篇 经济学
1 篇 文学
1 篇 艺术学

主题

590 篇 bioinformatics
264 篇 genomics
210 篇 proteins
176 篇 biological syste...
170 篇 computational bi...
169 篇 computational mo...
135 篇 biology computin...
120 篇 computational in...
114 篇 sequences
98 篇 dna
90 篇 gene expression
82 篇 feature extracti...
82 篇 artificial intel...
78 篇 databases
78 篇 machine learning
76 篇 predictive model...
74 篇 data mining
73 篇 diseases
65 篇 support vector m...
65 篇 humans

机构

14 篇 indian stat inst...
12 篇 jiangnan univ sc...
10 篇 bioinformatics r...
9 篇 indian stat inst...
8 篇 georgia state un...
7 篇 brock univ dept ...
6 篇 school of comput...
6 篇 ieee
6 篇 cent south univ ...
6 篇 univ guelph dept...
5 篇 univ south carol...
5 篇 tianjin univ col...
5 篇 georgia state un...
5 篇 univ bergamo dep...
5 篇 jilin univ sch a...
5 篇 osaka inst techn...
4 篇 tianjin univ col...
4 篇 computational sc...
4 篇 suzhou univ sci ...
4 篇 mathematics and ...

作者

17 篇 bandyopadhyay sa...
13 篇 rajapakse jagath...
13 篇 houghten sherida...
12 篇 daniel ashlock
11 篇 ashlock daniel
9 篇 j.c. rajapakse
9 篇 sheridan houghte...
9 篇 guo fei
8 篇 brown joseph ale...
8 篇 fogel gary b.
7 篇 tang jijun
7 篇 srinivas aluru
7 篇 shinn-ying ho
7 篇 nobile marco s.
7 篇 mohamad mohd sab...
6 篇 de rajat k.
6 篇 huseyin seker
6 篇 milone diego h.
6 篇 maji pradipta
6 篇 ding yijie

语言

1,458 篇 英文
22 篇 其他
4 篇 中文

检索条件"任意字段=IEEE Symposium on Computational Intelligence in Bioinformatics and Computational Biology"

共 1499 条记录，以下是901-910 订阅

全选清除本页清除全部题录导出标记到"检索档案"

详细简洁

排序：

Developmental biology from informatics point of view

Developmental biology from informatics point of view

引用

International symposium on computational intelligence and Informatics

作者： Sándor J. Piros Péter Korondi Department of Mechatronics Optics and Engineering Informatics Budapest University슠of슠Technology슠and슠Economics Budapest Hungary The Computer and Automation Research Institute Hungarian Academy of Sciences (ATOMKI) Budapest Hungary

There are several technical or technological field, which borrowed inspirations or hints from nature. This way it could be interesting to study, how a multicellular organism develops, by consecutive cell divisions, differentiations and proliferation, from a single cell. This development could be regarded as a decompression process of a highly compressed database. Following and mimicking this procedure we might be able to create a similar database or image processing transformation and compression method. The aim of our research is, finding the method how certain information is stored in the genome, which relates to the physical location and type of each cell of the body. Finding any such relationship, could help us to develop new image transformation and compression method.

关键词： Image coding bioinformatics Databases Organisms Informatics Genomics

来源：评论

学校读者我要写书评

暂无评论

Multi Level Clustering of Phylogenetic Profiles

Multi Level Clustering of Phylogenetic Profiles

引用

ieee symposium on bioinformatics and Bioengineering (BIBE)

作者： Fotis E. Psomopoulos Pericles A. Mitkas Intelligent Systems and Software Engineering Laboratory Informatics and Telematics Institute Thessaloniki Greece Department of Electrical and Computer Engineering Aristotle University of Thessaloniki Thessaloniki Greece

The prediction of gene function from genome sequences is one of the main issues in bioinformatics. Most computational approaches are based on the similarity between sequences to infer gene function. However, the availability of several fully sequenced genomes has enabled alternative approaches, such as phylogenetic profiles. Phylogenetic profiles are vectors which indicate the presence or absence of a gene in other genomes. The main concept of phylogenetic profiles is that proteins participating in a common structural complex or metabolic pathway are likely to evolve in a correlated fashion. In this paper, a multi level clustering algorithm of phylogenetic profiles is presented, which aims to detect inter- and intra-genome gene clusters.

关键词： Phylogeny bioinformatics Genomics Clustering algorithms Databases Proteins Biomedical engineering Intelligent systems computational intelligence Software engineering

来源：评论

学校读者我要写书评

暂无评论

Parallel applications employing pairwise computations on emerging architectures

Parallel applications employing pairwise computations on eme...

引用

ieee International symposium on Parallel and Distributed Processing Workshops and Phd Forum (IPDPSW)

作者： Abhinav Sarje Srinivas Aluru Department of Electrical and Computer Engineering Iowa State University Ames IA USA

ISBN: (纸本)9781424465330

Today's emerging architectures have higher levels of parallelism incorporated within a processor. They require efficient strategies to extract the performance they have to offer. In our work, we develop architecture-aware parallel strategies to perform various kinds of pairwise computations - pairwise genomic alignments, and scheduling large number of general pairwise computations with applications to computational systems biology and materials science. We present our schemes in the context of the IBM Cell BE, an example of a heterogeneous multicore, but are nevertheless applicable to any similar architecture, as well as general multicores with our strategies being cache-aware.

关键词： Computer applications Concurrent computing Computer architecture biology computing Multicore processing Parallel processing Genomics bioinformatics Processor scheduling computational systems biology

来源：评论

学校读者我要写书评

暂无评论

computational Framework for Microstructural Bone Dynamics Model and Its Evaluation

Computational Framework for Microstructural Bone Dynamics Mo...

引用

ieee symposium on bioinformatics and Bioengineering (BIBE)

作者： Taehyong Kim Woochang Hwang Aidong Zhang Murali Ramanathan Department of Computer Science and Engineering State University of New York Buffalo USA Department of Computer Science and Engineering State University of New York University at Buffalo Buffalo USA Department of Pharmaceutical Sciences State University of New York University at Buffalo Buffalo USA

Bones are firm and solid organs that form the skeleton of the body. Bone consists of living tissues with which bone remodeling occurs asynchronously at various sites and involves resorption by osteoclast, followed by formation of new bone by osteoblast. Although bone is a simple composite of a mineral structure, its structure highly contributes to the strength of the bone. In this paper, we develop a computational framework for microstructural bone dynamics modeling which is capable of quantitative assessment of bone mineral density and bone micro-architecture. Our paper focuses on bone microstructure and remodeling dynamics based on a bone network model. First, we generate a bone network based on our bone model reflecting bone microstructure. Next, we introduce a mathematical model of autocrine and paracrine interactions among osteoblast and osteoclast. It allows us to calculate cell population dynamics and changes in bone mass at multiple sites of bone remodeling. Last, we analyze two bone networks representing healthy bone and bone with osteoporosis with our evaluation measurements. Our study provides an initial framework of bone remodeling simulation that can explain experimental observations in bone biology to explore bone diseases such as osteoporosis.

关键词： Bones Minerals Microstructure Osteoporosis Solids Skeleton Mathematical model Biological system modeling Cells (biology) computational biology

来源：评论

学校读者我要写书评

暂无评论

TRAC: A Platform for Structure-Function Studies of NSS-Proteins Integrates Information from bioinformatics and Biomedical Literature

TRAC: A Platform for Structure-Function Studies of NSS-Prote...

引用

ieee symposium on bioinformatics and Bioengineering (BIBE)

作者： Lei Shi Marko Srdanovic Thijs Beuming Lucy Skrabanek Jonathan A. Javitch Harel Weinstein The HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute of Computational Biomedicine Weill Medical College of Cornell University New York NY USA Department of Physiology and Biophysics Weill Medical College of Cornell University New York NY USA Cornell University Joan and Sanford I Weill Medical College New York NY US Departments of Psychiatry and Pharmacology Center of Molecular Recognition College of Physicians and Surgeons Columbia University New York NY USA

To enable rigorous and reliable modeling of functional mechanisms of membrane proteins, the computational modeling and simulation approaches must take advantage, to the fullest extent possible, of the wealth of data obtained experimentally. This type of information makes it possible not only to construct rigorous molecular models and quantitative representations of function, but also to test, verify and refine them continuously. Among the proteins in the cell membrane, the family of Neurotransmitter: Sodium Symporter (NSS) exhibits highly complex mechanisms that involve multiple molecular states in the substrate and ion transport cycle. Due to their high biological and medical importance, experimental data for these systems is abundant, and efficient management of information from the literature and other relevant data sources promises to be very rewarding. We have developed an information management system (IMS) for data concerning the NSS proteins to enable retrieval, structured organization, and query of information available in the literature. The IMS supports the interplay between computational approaches and experimental studies of structure, function and physiological mechanisms of the NSS, and is of special utility in the integration of data of different types and various sources, and of the mechanistic understanding emerging from separate functional studies of individual members of the family.

关键词： bioinformatics Biomembranes Proteins computational modeling Biological system modeling Testing Cells (biology) Neurotransmitters Information management Health information management

来源：评论

学校读者我要写书评

暂无评论

Dynamic Complexity of the Temporal Transcriptional Regulation Program in Human Endotoxemia

Dynamic Complexity of the Temporal Transcriptional Regulatio...

引用

ieee symposium on bioinformatics and Bioengineering (BIBE)

作者： Tung T. Nguyen Panagiota T. Foteinou Ioannis P. Androulakis Steve E. Calvano Stephen F. Lowry BioMaPS Institute of Quantitative Biology & Department of Biomedical Engineering Rutgers University Piscataway NJ USA Department of Surgery Robert Wood Johnson Medical School University of Medicine and Dentistry of New Jersey New Brunswick NJ USA

Human endotoxemia is a well-accepted surrogate model for studying the acute inflammatory responses. In order to discover the complex underlying dynamics, identifying biologically relevant transcriptional regulators as well as their putative regulatory interactions with target genes is an essential step. However, prediction of relevant transcriptional regulators in higher eukaryotes remains a challenge both in silico and in vivo. In this study, we analyzed gene expression data from human blood leukocytes to extract four significant patterns of highly coexpressed genes that capture the essence of inflammatory phases. Upon identification of these patterns, a number of inflammation-specific pathways are selected by evaluating the enrichment of the corresponding subsets. Subsequently, statistically significant cis-regulatory modules (CRMs) are selected and decomposed into a list of relevant transcription factors (34 TFs) which are further validated from prior experiments and computational studies in literature. Additionally, our analysis also allows for the construction of a putative dynamic representation of the transcriptional regulatory program, making it become a critical enabler for unraveling regulatory interactions which is an essential step towards a quantification of dynamic transcriptional regulatory networks.

关键词： Humans Regulators Gene expression Biomedical engineering Pattern analysis Surgery Pathogens bioinformatics computational biology USA Councils

来源：评论

学校读者我要写书评

暂无评论

An Intelligent Multi-Agents Method for Study on Membrane Protein Interaction Network

An Intelligent Multi-Agents Method for Study on Membrane Pro...

引用

The 4th International Conference on bioinformatics and Biomedical Engineering(第四届ieee生物信息与生物医学工程国际会议 iCBBE 2010)

作者： Yi-Zhen Shen Yong-Sheng Ding College of Information Sciences and Technology Donghua University Shanghai 201620 P.R.China College of Information Sciences and Technology Donghua University Engineering Research Center of D

Membrane protein and its interaction network has become a novel research direction in bioinformatics. Multiple researches on these interactions can improve our understanding of diseases and provide the basis to revolutionize therapeutic treatments. In this paper, a novel membrane protein interaction network simulator is proposed for system biology studies by intelligent multi-agents method. We consider biological system as a set of active computational components interacting with each other and with an external environment. Then we can use the network simulator to construct membrane protein interaction networks. Interactions among small membrane protein interaction networks can emerge a large membrane protein interaction network which has its remarkable ability to accomplish a complex function or task. Based on the proposed approach, we find out that the membrane protein interaction network almost has the some dynamic and collective characters, such as small-world network, topological character, and hierarchical module structure. These characters of the membrane protein interaction network will be valuable for its relatively biological and medical studies.

关键词： Intelligent networks Biomembranes Proteins Biological system modeling computational modeling bioinformatics Diseases Systems biology computational intelligence Biological systems

来源：评论

学校读者我要写书评

暂无评论

Rapid RNA Folding: Analysis and Acceleration of the Zuker Recurrence

Rapid RNA Folding: Analysis and Acceleration of the Zuker Re...

引用

Annual ieee symposium on Field-Programmable Custom Computing Machines (FCCM)

作者： Arpith C. Jacob Jeremy D. Buhler Roger D. Chamberlain Department of Computer Science and Engineering Washington University of Saint Louis USA

RNA folding is a compute-intensive task that lies at the core of search applications in bioinformatics such as RNAfold and UNAFold. In this work, we analyze the Zuker RNA folding algorithm, which is challenging to accelerate because it is resource intensive and has a large number of variable-length dependencies. We use a technique of Lyngso to rewrite the recurrence in a form that makes polyhedral analysis more effective and use data pipelining and tiling to generate a hardware-friendly implementation. Compared to earlier work, processors in our array are more efficient and use fewer logic and memory resources. We implemented our array on a Xilinx Virtex 4 LX100-12 FPGA and experimentally verified a 103x speedup over a single core of a 3 GHz Intel Core 2 Duo CPU. The accelerator is also 17x faster than a recent Zuker implementation on a Virtex 4 LX200-11 FPGA and 12x and 6x faster respectively than an Nvidia Tesla C870 and GTX280 GPU. We conclude with a number of lessons in using FPGAs to implement arrays after polyhedral analysis. We advocate using polyhedral analysis to accelerate other dynamic programming recurrences in computational biology.

关键词： RNA Acceleration Field programmable gate arrays Biological system modeling Algorithm design and analysis Dynamic programming Sequences bioinformatics Logic arrays computational biology

来源：评论

学校读者我要写书评

暂无评论

Comparison of Co-temporal Modeling Algorithms on Sparse Experimental Time Series Data Sets

Comparison of Co-temporal Modeling Algorithms on Sparse Expe...

引用

ieee symposium on bioinformatics and Bioengineering (BIBE)

作者： Edward E. Allen James L. Norris David J. John Stan J. Thomas William H. Turkett Jr. Jacquelyn S. Fetrow Department of Mathematics Wake Forest University Winston Salem NC USA Department of Computer Science Wake Forest University Winston Salem NC USA Department of Computer Science Department of Physics Wake Forest University Winston Salem NC USA

Multiple approaches for reverse-engineering bio-logical networks from time-series data have been proposed in the computational biology literature. These approaches can be classified by their underlying mathematical algorithms, such as Bayesian or algebraic techniques, as well as by their time paradigm, which includes next-state and co-temporal modeling. The types of biological relationships, such as parent-child or siblings, discovered by these algorithms are quite varied. It is important to understand the strengths and weaknesses of the various algorithms and time paradigms on actual experimental data. We assess how well the co-temporal implementations of three algorithms, continuous Bayesian, discrete Bayesian, and computational algebraic, can 1) identify two types of entity relationships, parent and sibling, between biological entities, 2) deal with experimental sparse time course data, and 3) handle experimental noise seen in replicate data sets. These algorithms are evaluated, using the shuffle index metric, for how well the resulting models match literature models in terms of siblings and parent relationships. Results indicate that all three co-temporal algorithms perform well, at a statistically significant level, at finding sibling relationships, but perform relatively poorly in finding parent relationships.

关键词： Biological system modeling Bayesian methods Mathematical model biology computing Algebra Reverse engineering computational modeling Computer science Protein engineering Computer networks

来源：评论

学校读者我要写书评

暂无评论

Using special-purpose hardware to achieve a hundred-fold speedup in molecular dynamics simulations of proteins

Using special-purpose hardware to achieve a hundred-fold spe...

引用

ieee International symposium on Performance Analysis of Systems and Software

作者： David Shaw D. E. Shaw Research and Center of Computational Biology and Bioinformatics Columbia University USA

Summary form only given. Molecular dynamics (MD) simulation has long been recognized as a potentially transformative tool for understanding the behavior of proteins and other biological macromolecules, and for developing a new generation of precisely targeted drugs. Many biologically important phenomena, however, occur over timescales that have previously fallen far outside the reach of MD technology. We have constructed a specialized, massively parallel machine, called Anton, that is capable of performing atomic-level simulations of proteins at a speed roughly two orders of magnitude beyond that of the previous state of the art. The machine has now simulated the behavior of a number of proteins for periods as long as a millisecond -- approximately 100 times the length of the longest such simulation previously published -- revealing aspects of protein dynamics that were previously inaccessible to both computational and experimental study. The speed at which Anton performs these simulations is the result of a tightly coupled codesign process in which novel algorithms and architectural features were developed in concert, guided in large part by an iterative process of performance analysis and optimization.

关键词： Hardware Biological system modeling computational modeling Target recognition Protein engineering Molecular biophysics Drugs Biological information theory Pharmaceutical technology Parallel machines

来源：评论

学校读者我要写书评

暂无评论

没有更多数据了...

全选清除本页清除全部题录导出标记到“检索档案”

共150页 << < 87 88 89 90 91 92 93 94 95 96 > >>

检索报告对象比较合并检索0

隐藏清空

合并搜索

回到顶部

执行限定条件

内容：

评分：

请选择保存的检索档案：

请选择收藏分类：

订阅名称：

通借通还

温馨提示：

图书名称：

借书校区：

取书校区：

手机号码：

邮箱地址：

一卡通帐号：

电话和邮箱必须正确填写，我们会与您联系确认。

联系人：

所在院系：

联系邮箱：

联系电话：

内蒙古自治区呼和浩特市赛罕区大学西街235号邮编: 010021

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：